ClinVar Miner

Submissions for variant NM_001037.5(SCN1B):c.41-5C>T

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002938942 SCV003269328 likely benign Brugada syndrome 5 2022-07-11 criteria provided, single submitter clinical testing

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